| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278058 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
An efficient methodology for the preparation of α-hydroxyamides via boric acid-mediated addition of isonitriles onto aldehydes has been developed. The reaction of isonitriles with α-boronobenzaldehyde takes place under intramolecular catalysis conditions to provide functionalized benzoxaboroles.
Graphical abstractAn efficient methodology for the preparation of α-hydroxyamides via boric acid-mediated addition of isonitriles on to aldehydes has been developed. The reaction of isonitriles with α-boronobenzaldehyde takes place under intramolecular catalysis conditions to provide functionalized benzoxaboroles.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
J. Sravan Kumar, Subash C. Jonnalagadda, Venkatram R. Mereddy,